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HS Code |
611046 |
| Cas Number | 1824-81-3 |
| Molecular Formula | C6H8N2 |
| Molecular Weight | 108.14 g/mol |
| Iupac Name | 2-amino-6-methylpyridine |
| Appearance | Light yellow to brown solid |
| Boiling Point | 258-260 °C |
| Melting Point | 34-38 °C |
| Density | 1.085 g/cm³ |
| Solubility In Water | Slightly soluble |
| Flash Point | 128 °C |
| Purity | Typically ≥98% |
| Synonyms | 6-Methyl-2-pyridinamine |
| Smiles | CC1=NC(=CC=C1)N |
| Storage Temperature | Store at 2-8 °C |
| Refractive Index | 1.609 |
As an accredited 2-Amino-6-Methylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle with secure screw cap, labeled “2-Amino-6-Methylpyridine, 99%, 100 grams.” Includes hazard symbols and safety information. |
| Shipping | 2-Amino-6-Methylpyridine should be shipped in a tightly sealed container, protected from moisture and incompatible substances. It must be clearly labeled, packed according to regulations for hazardous chemicals, and accompanied by the appropriate Safety Data Sheet (SDS). Transport in compliance with local, national, and international guidelines for chemical shipments. |
| Storage | 2-Amino-6-methylpyridine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents. Protect it from moisture and direct sunlight. Clearly label the container and keep it away from sources of ignition, heat, or open flame. Use appropriate chemical storage practices and follow safety protocols. |
Applications of 2-Amino-6-Methylpyridine in Industrial ManufacturingOur production expertise ensures the consistent quality supply of 2-Amino-6-Methylpyridine to support critical downstream industries. Below, we outline the principal industrial applications, each with detailed integration and compliance information relevant to manufacturing environments. 1. Pharmaceutical Intermediates for Antihypertensive API Synthesis2-Amino-6-Methylpyridine functions as a key intermediate in the multistep synthesis of antihypertensive active pharmaceutical ingredients, including Amlodipine and its analogs. Manufacturers incorporate this compound into closed batch or continuous synthetic routes, facilitating selective modifications on the pyridine ring for subsequent steps. QC teams regularly monitor trace impurities that could impact the API profile, and process engineers fine-tune reaction parameters to maximize conversion while ensuring regulatory compliance, particularly concerning nitrosamine precursors. Integration into the pharmaceutical pipeline requires full traceability and validation documentation per commercial drug substance requirements. Industry compliance standards
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2. Agrochemical Synthesis for Pyridine-Based Pesticide Active IngredientsIn crop protection manufacturing, this methylated aminopyridine is widely utilized as a pyridine building block in the synthesis of selective herbicides and insecticides that target resistant weed biotypes. Downstream processors integrate it into catalytic alkylation or coupling reactions for the construction of complex heterocyclic pesticide backbones, paying careful attention to process yield and impurity management required by regulatory dossiers. The material’s purity influences both synthetic throughput and the stability profile of the formulated pesticide, necessitating validated cleaning and segregation protocols in multipurpose chemical plants. Industry compliance standards
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3. Synthesis of Specialty Dyes and PigmentsThis compound acts as a nitrogenous heterocycle precursor in the manufacture of custom high-performance dyes for fiber, paper, and polymer applications. Specialized dye houses use it in diazotization-condensation sequences or as a coupling fragment in azo and anthraquinone dye synthesis. Operators maintain strict procedural controls to prevent cross-contamination between dye color series, and particle size distribution is closely monitored in the finished pigment to ensure consistency in coloration and dispersion when incorporated into end-user formulations. Industry compliance standards
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4. API Intermediate in Central Nervous System (CNS) Drug Production2-Amino-6-Methylpyridine serves as a foundational building block in the multistep synthesis of certain CNS-active pharmaceuticals, most notably as an intermediate for anticonvulsant and antipsychotic drugs. Strict GMP protocols are observed from raw material receipt through to intermediate isolation and downstream coupling reactions, particularly as the chemical structure influences both the pharmacokinetics and impurity profiles of final CNS APIs. All upstream and midstream R&D and QA functions validate assay, residual solvent, and genotoxic impurity levels at each synthetic stage. Industry compliance standards
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5. Heterocyclic Ligand Synthesis for Advanced CatalysisLeading catalyst and ligand manufacturers utilize 2-Amino-6-Methylpyridine for fabricating custom heterocyclic ligand systems deployed in pharmaceutical and fine chemical syntheses. The compound is introduced at initial stages to create bidentate or tridentate ligands via controlled N-functionalization, where the electron-donating amino group facilitates metal complexation. Chemists closely control batch parameters and analytical qualification, since minor variations in the feedstock can alter the coordination environment and hence the activity profile of the final catalytic system. Industry compliance standards
Typical usage ratio
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In the family of methyl-substituted pyridines, 2-Amino-6-Methylpyridine (CAS 1824-81-3) offers chemists a unique combination of chemical reactivity and selectivity, owing to its bivalent structure—an amino group at the 2-position and a methyl group at the 6-position. We manufacture this compound because of its growing relevance across pharmaceuticals, agrochemicals, and specialty materials. The model we keep in continuous production is the crystalline solid, with a purity reaching up to 99.5% (GC), yielding a pale to off-white powder typically packed in fiber drums with double linings to minimize moisture exposure and contamination.
Over decades of hands-on experience, we have learned that end-users pursue a very particular set of product traits in 2-Amino-6-Methylpyridine: high purity, consistent particle size, and batch-to-batch reproducibility. Production at scale forces every flaw to the surface—micro-level impurities, inconsistent drying, and even how the material cakes after sitting in storage—issues that rarely appear in lab-scale runs. Our synthesis relies on catalytic amination, drawing from years of internal process development, with quality monitored at every reaction stage. Chemists in our operations have tuned this process to minimize side-products, especially those introducing N-oxide or N-methylpyridine isomers. Maintaining purity at this level comes from persistent hands-on control, not from theory.
Formulators and R&D teams come to us describing failures: a stalled downstream synthesis, unexpected impurities hampering separation, or yield drops caused by trace byproducts from upstream raw materials. In intermediate chemistry, 2-Amino-6-Methylpyridine drives a set of transformations you won’t coax out of other pyridines. Its amino group’s position relative to the ring nitrogen supports electrophilic substitution and specialized coupling reactions. For example, in pharmaceutical discovery, our product often ends up in the core or as a building block in kinase inhibitors and central nervous system drug candidates. The 6-methyl substituent changes the electron density so that halogenation, diazotization, and Suzuki couplings go to plan with fewer off-path reactions.
Agrochemical chemists leverage its profile to engineer selectivity in crop protection molecules. Broadleaf herbicide libraries often draw from substituted aminopyridines, with methyl positioning tuned to fine-tune environmental breakdown rates, a feature that 2-Amino-6-Methylpyridine supports better than its 4- or 3-methyl counterparts. In dye and pigment research, customers consider it for high-stability azo dye precursors, especially when both color fastness and lightfastness are demanded.
Process engineers care most about product purity and moisture control. Residual water—in concentrations above 0.3%—can alter reactivity, lead to unplanned hydrolysis, and in the worst cases, derail pilot-plant or scale-up campaigns. Users tell us about lost batches and failed pilot runs blamed on variable water content from other suppliers. Our team dries every batch under vacuum down to under 0.15% water, with samples sealed in air-tight, inert packaging to retain this low threshold through transit and storage. The inherent stability of 2-Amino-6-Methylpyridine means careful packing pays dividends for our partners.
The choices in the aminopyridine family boggle younger chemists: 2-Aminopyridine, 3-Aminopyridine, their methyl-substituted cousins at positions 3, 4, or 5—all seem similar on paper. But with experience in both manufacturing and downstream feedback, our prescription remains: don’t treat these as interchangeable. The methyl group right at the 6-position blocks some routes of ring activation and governs steric environment on the pyridine nitrogen, letting users direct selectivity in reactions, from Buchwald couplings to heteroaryl halide displacements.
For instance, compared to 2-amino-3-methylpyridine, our product’s unique methyl placement at the 6-position reduces ring tautomerization and protects amine activity in high-temperature or basic conditions. Customers using the 4-methyl analogs see greater N-oxide formation and sluggish coupling rates—not a problem in our material. The electron-donating methyl increases nucleophilicity on the ring’s meta positions, teaching process chemists to plan their reaction sequences with more control. This subtlety may seem minor in theory, but in real-world production, a day’s lost output—or worse, an off-spec intermediate held up for weeks—quickly proves otherwise.
Scaling up aminopyridine production is more than moving glassware into a reactor. The basicity of the 2-amino group draws moisture and carbon dioxide from the atmosphere. For drum storage, we keep everything under dry nitrogen. During packing, careful sieving minimizes fine dust, which could otherwise compromise operator safety. Colleagues in formulation plants have praised the dust-free, free-flowing quality, calling out how some competitors’ lots solidify into clumps after just a week on the shelf.
Inside our process, purification is not a one-and-done step. Starting material purity sets the ceiling on end-quality, but subtle process tricks—multiple re-crystallizations using proprietary solvents, low-temperature batch settling, and inline moisture analysis—bring final purity up to our target every time. Each step is adjusted using data from organic synthesis teams working at bench and pilot scale, and minor changes are tested on batch sub-samples by QA chemists. The focus isn’t just theoretical: some manufacturing tweaks shaved days off typical lead times for our customers, simply because we reduced labor downstream and simplified filtration.
Customers rarely question purity when quality stays consistent. But changes—even percentage points in impurity, shifts in color, or caking after transit—trigger production headaches and lost confidence. From the start, our commitment has centered on conversations with users, from process development scientists to warehouse staff who handle the product. Hundreds of tons passed through our hands, yet we still run in-process controls at every scale-up, using HPLC and NMR alongside traditional titration and melting point analysis.
Minimizing trace impurities keeps regulatory approvals on track for our customers in pharma and agrochemicals. Even trace levels of metal ions or polycyclic side-products can threaten product registrations, drive up analytical costs, or force additional purification steps. We seek raw material sources with proven, long-term reliability, choosing suppliers not by price alone but through consistent upstream audit trails. For our buyers, a reliable supplier of 2-Amino-6-Methylpyridine means fewer sleepless nights tracking down equipment corrosion, contamination, or sudden reaction failures.
Years in chemical manufacturing have taught us caution is earned the hard way. We have rerun entire series of batches based on a minute shift in GC peaks or uncharacteristic melting range. Rather than rely on certificates alone, we encourage new users to request multi-point samples and trial quantities before full-scale commitments. Feedback from batch trials—whether it comes from a Japanese pharma major or a niche agricultural R&D group—drives our own process modifications, not just incremental adjustments but sometimes major overhauls of crystallization or drying protocols.
Our engagement with research teams reaches beyond technical sheets. We have helped users address unplanned deposits in downstream reactors by identifying trace amines, then re-optimizing filtration and drying. Not every maker can justify this kind of hands-on feedback loop, but for us, each improvement pays off in tighter process control and stronger long-term relationships.
Compliance with modern good manufacturing practice runs deep in our operation. Quality management isn’t an abstract, far-away checklist—auditors stand on our production floors, verify lot-traceability, and check that each batch ships with full spectral and microanalysis data. Working toward ISO certification influenced how we train every technician, calibrate analytical instruments, and store environmental monitoring logs. End-users in tightly regulated domains—pharma synthesis, API intermediates, crop science—require this, and maintaining these standards underpins every kilogram for export.
Our documentation carries actual batch records, full spectral data—^1H and ^13C NMR, IR, GC/MS readouts—plus replicates during analysis to guarantee accuracy. Regular external audits, both scheduled and random, continuously shape our process improvement plans, not as interruptions but as a core requirement. Regulatory shifts in allowable impurity levels or banned processing reagents ripple back through our whole supply chain; we treat early awareness and transparent communication as practical needs, not empty promises.
Every producer faced supply chain shocks in recent years. Pre-pandemic, conversations focused on cost and single-source optimization. Since late 2020, everyone’s vocabulary evolved—buffer inventory, dual-sourcing, and local warehousing matter as much as rate and purity. We ramped up buffer stock and worked with key global partners to guarantee delivery windows, coordinating cargoes with shipping agents who understand the hazards and shelf-life limits of fine chemicals like 2-Amino-6-Methylpyridine.
We learned painful lessons about relying on any single raw material source. Today, our raw pyridine base and amination reagents come from multiple pre-approved global partners, with analytical pre-approval on every lot before release to our reactors. Regular communication with logistics and warehouse teams helps us keep clients informed—no one likes surprises on critical-path projects. Rather than chase minimum costs, we place steady performance and ready availability above all.
Chemicals don’t disappear at the end of a process. Our experience showed us that responsible manufacturing means capturing and treating all effluents from 2-Amino-6-Methylpyridine production. Organic nitrogen and pyridine derivatives have lingering ecological footprints: improper wastewater handling causes contamination, drives up regulatory attention, and weakens license renewals.
We invested heavily in in-house effluent treatment—adsorptive resin beds for amine residues, activated carbon for trace organics, robust pH neutralization—and run life-cycle assessments to minimize hazardous waste streams. Recent upgrades let us recover and recycle a significant share of processing solvent, cutting our disposal volumes compared to previous years. Customers aiming for greener supply chains regularly audit our reporting and tour our treatment stations to ensure true compliance.
The value of such investments outweighs their cost over time. As market demand shifts towards more sustainable sourcing, we see direct improvements in community relations and worker retention arising from our environmental stewardship.
Over years of partnerships with labs and manufacturing firms, we gain an insider’s view of the practical use of 2-Amino-6-Methylpyridine. It isn’t just about the bulk order and a certificate of analysis. We suggest, for labs moving up to kilo-scale, store drums in a dry area, out of direct sunlight, and limit the container’s exposure to open air. Plan for a quick clean-up if spills occur, as the powder’s volatility can irritate sensitive nasal or respiratory systems.
If using the product as a registered intermediate for regulated substances, collect all batch numbers, analytical data, and batch retention samples for post-hoc traceback. For teams using it in pilot programs, draw a small batch sample before full release into active synthesis so you can spot off-spec events early. Over our long run in this field, these precautions have prevented countless production headaches and averted scale-up disasters even before they began.
Our relationship to each drum of 2-Amino-6-Methylpyridine doesn’t end at the shipping dock. Field feedback—an off-color batch observed by a formulator, a process engineer flagging slower filtration, or a researcher spotting a change in melting point—always comes back to our technical team. The most valuable improvements spring up from these reports, not top-down mandates.
Regular plant meetings bring together operators, analysts, and packers to share their hands-on knowledge—how a shift in raw material supplier triggered more sticky product, or how a new filter material sharpened drying rates and reduced fines. Continuous investment in practical site training means employees recognize subtle changes in product feel, lumping tendency, or packing sound that no machine alone catches. We believe this ‘shop floor intelligence’ belongs as much in modern quality assurance as any digital record.
Choosing 2-Amino-6-Methylpyridine from a direct manufacturer brings advantages often overlooked in price-driven procurement. We offer a real relationship built on technical support, lab-to-plant troubleshooting, and willingness to adapt to unusual requests. Experienced plant chemists understand the pain points involved in switching suppliers or qualifying new lots. Early access to our own internal test reports, as well as historical data on stability and performance, saves our clients days or even weeks during scale transfer or quality disputes.
Our focus rests on actual utility: reproducibility in large-scale settings, low residual moisture for water-sensitive chemistry, and a packaging standard tuned for real transit environments. Custom pack sizes, tailored drying protocols on request, and expedited sampling embody the flexibility we bring as a chemical producer, not just a reseller or spec-sheet intermediary.
As applications broaden and new regulatory or market demands emerge, we constantly revisit our manufacturing and QA approaches for 2-Amino-6-Methylpyridine. Intellectual property in this space continues to expand, with more routes incorporating this molecule into drug intermediates, ligand libraries for catalysis, or as linkers in next-generation materials.
Our goal stays rooted in continuous improvement, taking the lessons from each batch, each customer report, and each analytical result as drivers for product evolution. The next generation of this compound—whether it involves further drying refinements, particle size tuning, or new purity standards—will reflect both global best practices and the honest, technical feedback from the clients and operators who use it every week.